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The effect of saline lock on prevention of phlebitis

Not Applicable
Conditions
Phlebitis.
Vascular complications following infusion, transfusion and therapeutic injection
Registration Number
IRCT2014062118176N1
Lead Sponsor
Research Deputy of Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
150
Inclusion Criteria

adult patients (Older than 18 years old) admitted to the medical-surgical wards that will hospitalized at least three days after surgery; patients with peripheral intravenous catheter in the upper limb (on the forearm) and patients who were willing to participate.
Exclusion criteria: patients who had any underlying blood disorders (eg, hemophilia, diabetes, etc); patients who receiving anticoagulant therapy (heparin, warfarin, Plavix, etc); patients who receiving IV potassium chloride; patients who receiving continuous intravenous fluid therapy; replacement of the catheter for any reason other than phlebitis; discharged or died during the study period; emergency situation that requires immediate medical or nursing interventions, such as cardiopulmonary resuscitation.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Phlebitis. Timepoint: 24-48-72 hours, respectively, after the pre-test. Method of measurement: Visual Analogue Scale phlebitis.
Secondary Outcome Measures
NameTimeMethod
Infiltration and the patency of the catheter. Timepoint: respectively, 24-48-72 hours after the pre-test. Method of measurement: Observation checklist and visual analogue scale infiltration.
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